Evidence map›Paper›PMID 42157799›Full record

ArticleIranian journal of pharmaceutical research : IJPR

Gamabufotalin Suppresses Colorectal Cancer Growth via Oxidative Stress-Induced Apoptosis and DNA Synthesis Inhibition.

Hui Nie, Anfang Cui, Zhicheng Sun, Zhaoyang Li, Jianhua Guo, Shuhao Fan, Xiangchen Wang, Yong Xia

Abstract read
In one paragraph

Article in Iranian journal of pharmaceutical research : IJPR. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Hui Nie *School of Pharmacy, Shandong First Medical University (Shandong Academy of Medical Sciences), Jinan, China.
Anfang Cui *College of Basic Medicine, Jining Medical University, Jining, China.
Zhicheng SunKey Laboratory for Chronic Non-communicable Diseases, Institute of Precision Medicine, College of Medical Engineering, Jining Medical University, Jining, China.
Zhaoyang LiKey Laboratory for Chronic Non-communicable Diseases, Institute of Precision Medicine, College of Medical Engineering, Jining Medical University, Jining, China.
Jianhua GuoKey Laboratory for Chronic Non-communicable Diseases, Institute of Precision Medicine, College of Medical Engineering, Jining Medical University, Jining, China.
Shuhao FanKey Laboratory for Chronic Non-communicable Diseases, Institute of Precision Medicine, College of Medical Engineering, Jining Medical University, Jining, China.
Xiangchen WangSchool of Pharmacy, Shandong First Medical University (Shandong Academy of Medical Sciences), Jinan, China.
Yong XiaKey Laboratory for Chronic Non-communicable Diseases, Institute of Precision Medicine, College of Medical Engineering, Jining Medical University, Jining, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Colorectal cancer (CRC) continues to be a major cause of cancer-related mortality worldwide, creating an urgent need to develop novel therapeutic agents that are both highly effective and minimally toxic. Gamabufotalin (GA), a bioactive bufadienolide compound, has shown promising antitumor potential, including against CRC; however, its precise mechanisms of action in CRC remain incompletely understood. Objectives: The aim of this study was to investigate the therapeutic effect of GA on CRC and explore the underlying molecular mechanisms. Methods: A combination of in vitro and in vivo approaches was employed, including cell viability assays, colony formation, EdU incorporation, cell cycle and apoptosis analyses by flow cytometry, ROS and mitochondrial membrane potential detection, as well as integrated transcriptomic and proteomic profiling. The in vivo antitumor efficacy was further validated in a nude mouse xenograft model. Results: Gamabufotalin exhibited potent, dose-dependent anti-CRC activity in vitro (IC Conclusions: Gamabufotalin selectively and potently inhibits CRC through dual mechanisms: Inducing ROS-mediated apoptosis and suppressing proliferation. With a favorable therapeutic index and defined molecular targets, GA represents a promising candidate for CRC therapy.

Indexed as

ApoptosisColorectal CancerDNA SynthesisGamabufotalinOxidative Stress

Identifiers

PMID42157799
PMCPMC13181813

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